[Histonet] chicken EGFP aby

2010-10-07 Thread Susan Travers
Does anyone have experience with detecting EGFP with some of the current aby's 
made in chicken?  We have used aby's from both AVES labs and Millipore with 
negative results. In both cases we used the biotinylated secondary aby from 
AVES followed by a fluorescent streptavidin.  Absolutely no staining.  

Using the same tissue, we were able to use a different aby made in rabbit and 
it worked great. However, because of double-labeling needs we'd really like to 
get the chicken to work.

Perhaps someone has experience or insights?

Thanks!
Susan Travers
Division of Oral Biology
College of Dentistry
The Ohio State University
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Re: [Histonet] chicken EGFP aby

2010-10-07 Thread Adam .
I've had good luck using Abcam's chicken polyclonal:
http://www.abcam.com/GFP-antibody-ab13970.html

I use a directly conjugated secondary, and the staining is usually pretty
bright. But then again, my GFP expression is high.

Adam

On Thu, Oct 7, 2010 at 7:44 AM, Susan Travers traver...@osu.edu wrote:

 Does anyone have experience with detecting EGFP with some of the current
 aby's made in chicken?  We have used aby's from both AVES labs and Millipore
 with negative results. In both cases we used the biotinylated secondary aby
 from AVES followed by a fluorescent streptavidin.  Absolutely no staining.

 Using the same tissue, we were able to use a different aby made in rabbit
 and it worked great. However, because of double-labeling needs we'd really
 like to get the chicken to work.

 Perhaps someone has experience or insights?

 Thanks!
 Susan Travers
 Division of Oral Biology
 College of Dentistry
 The Ohio State University

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[Histonet] Training

2010-10-07 Thread Carter, Kendra
Does anyone know of any GLP training in El Paso, TX?

Kendra Leigh Carter
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Subject: Histonet Digest, Vol 83, Issue 6

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Today's Topics:

   1. RE: Helicobacter pylori (Laurie Colbert)
   2. RE: AChE fiber staining protocoll? (szi...@bio.u-szeged.hu)
   3. RE: Helicobacter pylori (Weems, Joyce)
   4. PAS STAIN (Diana McCaig)
   5. Histokinette 2000 (Biedermann, JoAnn)
   6. RE: PAS STAIN (Rathborne, Toni)
   7. Query Special Stainers (Joanne Clark)
   8. Re: Helicobacter pylori (Brandi Higgins)
   9. AW: [Histonet] PAS STAIN (Gudrun Lang)
  10. Where to buy Michels  RE: [Histonet] DIF Transport Media
  (gayle callis)
  11. RE: Query Special Stainers (Mahoney,Janice A)
  12. RE: PAS STAIN (gayle callis)
  13. RE: Query Special Stainers (Marcia Funk)
  14. PAS staining (Janet Keeping)


--

Message: 1
Date: Wed, 6 Oct 2010 07:48:25 -0700
From: Laurie Colbert laurie.colb...@huntingtonhospital.com
Subject: RE: [Histonet] Helicobacter pylori
To: Kathy M. Gorham km...@grh.org,
histonet@lists.utsouthwestern.edu
Message-ID:

57be698966d5c54eae8612e8941d768309a5a...@exchange3.huntingtonhospital.com

Content-Type: text/plain;   charset=us-ascii

We basically do a dif quik stain.  I buy a kit called Three Step Stain
from Cardinal. The total staining process takes about 1 minute.
Laurie Colbert

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Kathy M.
Gorham
Sent: Wednesday, October 06, 2010 7:20 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Helicobacter pylori

Good Morning Histo land. I would like to know what others are using for
a special stain for Helicobacter pylori not IHC. Do you use a kit? From
where? Make up your own?  Procedure. Thanks you.  You have always been
so helpful. Kathy Gorham H.T.


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--

Message: 2
Date: Wed, 06 Oct 2010 17:00:35 +0200
From: szi...@bio.u-szeged.hu
Subject: RE: [Histonet] AChE fiber staining protocoll?
To: Houston, Ronald ronald.hous...@nationwidechildrens.org
Cc: histonet@lists.utsouthwestern.edu
histonet@lists.utsouthwestern.edu
Message-ID: 20101006170035.j2waztulso448...@webmail.u-szeged.hu
Content-Type: text/plain;   charset=ISO-8859-2; DelSp=Yes;
format=flowed

Idézet (Houston, Ronald ronald.hous...@nationwidechildrens.org):


Thank you for the answer. We will try this protocol and i will reply  
the results.
Csaba Szigeti

 I have had great success in fine fibers with the modification of   
 Martucciello et al, Eur J Pediatr Surg 2001; 11: 300-304, but only   
 in 15 micron intestine sections, so I do not know how it will   
 transpose to brain studies and the thicker sections

 Ronnie Houston
 Anatomic Pathology Manager
 Nationwide Children's Hospital
 Columbus OH 43205
 (614) 722 

[Histonet] problems with staining IHC

2010-10-07 Thread srishan
Hi All,

Our pathologists have made a complain that the staining of slides have 
been a problem.  Same antibodies which stain one day does not work the 
following day.  This has been going on for a few months.  When we repeat 
stain they either work or not work and we have been sending them to 
reference labs. 

Our tech support person was here and told us that the slides ( fisher plus 
slides) have been a problem with some of her customers.  Meanwhile our 
surrounding labs which are using the same slides have no issues.  She 
showed us how the reagents were not spreading properly on the slides. 

Is anyone confronted this issue?  If so,  how was it solved? 

Thanks in advance.

Mala Srishan
Supervisor, Histology
Holy Name Medical Center
Teaneck NJ 07666


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Magnet Recognition for Excellence in Patient Care, American Nurses 
Credentialing Center

100 Best Places to Work in Healthcare, Ranked Fourth Nationally by Modern 
Healthcare

Best Places to Work in New Jersey, NJBIZ

Awards for Emergency, Outpatient and Inpatient Service Excellence, J.D. 
Power

Distinguished Hospital Awards for Clinical Excellence, HealthGrades

Excellence Awards for Stroke, Gastrointestinal and Pulmonary Care, 
HealthGrades

Best in Value Award, Data Advantage, LLC

Chest Pain Center Accreditation, Society of Chest Pain Centers

Primary Stroke Center Designation, The Joint Commission and NJ Department 
of Health and Human Services


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RE: [Histonet] problems with staining IHC

2010-10-07 Thread Settembre, Dana
Are you staining by hand or are you automated?
Dana Settembre
University Hospital
Newark, NJ

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of 
sris...@mail.holyname.org
Sent: Thursday, October 07, 2010 10:32 AM
To: histonet-boun...@lists.utsouthwestern.edu; Histonet@lists.utsouthwestern.edu
Subject: [Histonet] problems with staining IHC

Hi All,

Our pathologists have made a complain that the staining of slides have 
been a problem.  Same antibodies which stain one day does not work the 
following day.  This has been going on for a few months.  When we repeat 
stain they either work or not work and we have been sending them to 
reference labs. 

Our tech support person was here and told us that the slides ( fisher plus 
slides) have been a problem with some of her customers.  Meanwhile our 
surrounding labs which are using the same slides have no issues.  She 
showed us how the reagents were not spreading properly on the slides. 

Is anyone confronted this issue?  If so,  how was it solved? 

Thanks in advance.

Mala Srishan
Supervisor, Histology
Holy Name Medical Center
Teaneck NJ 07666


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Credentialing Center

100 Best Places to Work in Healthcare, Ranked Fourth Nationally by Modern 
Healthcare

Best Places to Work in New Jersey, NJBIZ

Awards for Emergency, Outpatient and Inpatient Service Excellence, J.D. 
Power

Distinguished Hospital Awards for Clinical Excellence, HealthGrades

Excellence Awards for Stroke, Gastrointestinal and Pulmonary Care, 
HealthGrades

Best in Value Award, Data Advantage, LLC

Chest Pain Center Accreditation, Society of Chest Pain Centers

Primary Stroke Center Designation, The Joint Commission and NJ Department 
of Health and Human Services


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RE: [Histonet] problems with staining IHC

2010-10-07 Thread Blazek, Linda
Hi Mala,
I had this same problem.  It was solved by adding Tween to the buffer.  It made 
the reagents flow much better over the slides.  Also before you stain, put the 
slides in a rinse of buffer/tween and agitate them for about 30 seconds.

Linda


Linda Blazek HT (ASCP)
Manager/Supervisor
GI Pathology of Dayton
Digestive Specialists, Inc
7415 Brandt Pike
Huber Heights, OH 45424
Phone: (937) 396-2623
Email: lbla...@digestivespecialists.com



-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of 
sris...@mail.holyname.org
Sent: Thursday, October 07, 2010 10:32 AM
To: histonet-boun...@lists.utsouthwestern.edu; Histonet@lists.utsouthwestern.edu
Subject: [Histonet] problems with staining IHC

Hi All,

Our pathologists have made a complain that the staining of slides have 
been a problem.  Same antibodies which stain one day does not work the 
following day.  This has been going on for a few months.  When we repeat 
stain they either work or not work and we have been sending them to 
reference labs. 

Our tech support person was here and told us that the slides ( fisher plus 
slides) have been a problem with some of her customers.  Meanwhile our 
surrounding labs which are using the same slides have no issues.  She 
showed us how the reagents were not spreading properly on the slides. 

Is anyone confronted this issue?  If so,  how was it solved? 

Thanks in advance.

Mala Srishan
Supervisor, Histology
Holy Name Medical Center
Teaneck NJ 07666


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Holy Name Medical Center is the recipient of:

Magnet Recognition for Excellence in Patient Care, American Nurses 
Credentialing Center

100 Best Places to Work in Healthcare, Ranked Fourth Nationally by Modern 
Healthcare

Best Places to Work in New Jersey, NJBIZ

Awards for Emergency, Outpatient and Inpatient Service Excellence, J.D. 
Power

Distinguished Hospital Awards for Clinical Excellence, HealthGrades

Excellence Awards for Stroke, Gastrointestinal and Pulmonary Care, 
HealthGrades

Best in Value Award, Data Advantage, LLC

Chest Pain Center Accreditation, Society of Chest Pain Centers

Primary Stroke Center Designation, The Joint Commission and NJ Department 
of Health and Human Services


 Warning: The information contained in this message is privileged and 
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RE: [Histonet] problems with staining IHC

2010-10-07 Thread Sebree Linda A
What kind of stainers are you using and is it happening on all your
stainers?  Or are you staining by hand? 


Linda A. Sebree
University of Wisconsin Hospital  Clinics
IHC/ISH Laboratory
DB1-223 VAH
600 Highland Ave.
Madison, WI 53792
(608)265-6596


-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of
sris...@mail.holyname.org
Sent: Thursday, October 07, 2010 9:32 AM
To: histonet-boun...@lists.utsouthwestern.edu;
Histonet@lists.utsouthwestern.edu
Subject: [Histonet] problems with staining IHC

Hi All,

Our pathologists have made a complain that the staining of slides have 
been a problem.  Same antibodies which stain one day does not work the 
following day.  This has been going on for a few months.  When we repeat

stain they either work or not work and we have been sending them to 
reference labs. 

Our tech support person was here and told us that the slides ( fisher
plus 
slides) have been a problem with some of her customers.  Meanwhile our 
surrounding labs which are using the same slides have no issues.  She 
showed us how the reagents were not spreading properly on the slides. 

Is anyone confronted this issue?  If so,  how was it solved? 

Thanks in advance.

Mala Srishan
Supervisor, Histology
Holy Name Medical Center
Teaneck NJ 07666


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Holy Name Medical Center is the recipient of:

Magnet Recognition for Excellence in Patient Care, American Nurses 
Credentialing Center

100 Best Places to Work in Healthcare, Ranked Fourth Nationally by
Modern 
Healthcare

Best Places to Work in New Jersey, NJBIZ

Awards for Emergency, Outpatient and Inpatient Service Excellence, J.D. 
Power

Distinguished Hospital Awards for Clinical Excellence, HealthGrades

Excellence Awards for Stroke, Gastrointestinal and Pulmonary Care, 
HealthGrades

Best in Value Award, Data Advantage, LLC

Chest Pain Center Accreditation, Society of Chest Pain Centers

Primary Stroke Center Designation, The Joint Commission and NJ
Department 
of Health and Human Services


 Warning: The information contained in this message is privileged
and 
CONFIDENTIAL and is intended only for the use of the addressee above. If

you are not the intended recipient, you are hereby notified that any 
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on 
the content of this message is strictly prohibited. If you have received

this communication in error, please notify the sender by replying to
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Re: [Histonet] problems with staining IHC

2010-10-07 Thread Jan Shivers

Mala,

If your main problem is that the reagents aren't spreading across your 
slides, I agree that you should put Tween 20 (0.05% per volume) in all of 
your rinse buffers between steps, regardless of if you do your IHC stains 
manually or with an autostainer.


If this doesn't solve the problem, post your method on histonet so that we 
know more about your procedure steps and can send additional advice.


Jan Shivers
UMN Vet Diag Lab

- Original Message - 
From: sris...@mail.holyname.org
To: histonet-boun...@lists.utsouthwestern.edu; 
Histonet@lists.utsouthwestern.edu

Sent: Thursday, October 07, 2010 9:32 AM
Subject: [Histonet] problems with staining IHC



Hi All,

Our pathologists have made a complain that the staining of slides have
been a problem.  Same antibodies which stain one day does not work the
following day.  This has been going on for a few months.  When we repeat
stain they either work or not work and we have been sending them to
reference labs.

Our tech support person was here and told us that the slides ( fisher plus
slides) have been a problem with some of her customers.  Meanwhile our
surrounding labs which are using the same slides have no issues.  She
showed us how the reagents were not spreading properly on the slides.

Is anyone confronted this issue?  If so,  how was it solved?

Thanks in advance.

Mala Srishan
Supervisor, Histology
Holy Name Medical Center
Teaneck NJ 07666


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Holy Name Medical Center is the recipient of:

Magnet Recognition for Excellence in Patient Care, American Nurses
Credentialing Center

100 Best Places to Work in Healthcare, Ranked Fourth Nationally by Modern
Healthcare

Best Places to Work in New Jersey, NJBIZ

Awards for Emergency, Outpatient and Inpatient Service Excellence, J.D.
Power

Distinguished Hospital Awards for Clinical Excellence, HealthGrades

Excellence Awards for Stroke, Gastrointestinal and Pulmonary Care,
HealthGrades

Best in Value Award, Data Advantage, LLC

Chest Pain Center Accreditation, Society of Chest Pain Centers

Primary Stroke Center Designation, The Joint Commission and NJ Department
of Health and Human Services


 Warning: The information contained in this message is privileged and
CONFIDENTIAL and is intended only for the use of the addressee above. If
you are not the intended recipient, you are hereby notified that any
disclosure, copying, distribution, or taking of any action in reliance on
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RE: [Histonet] problems with staining IHC

2010-10-07 Thread Tim Higgins
Hi Mala,

We've used the Fisher superfrost plus slides for years and have never had
that issue, it sounds more like you need to add some Tween to your buffer.
That will help the solutions spread along your slide.

Hope that helps. 


Thanks,
 
Timothy Higgins, HT(ASCP) QIHC

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of
sris...@mail.holyname.org
Sent: Thursday, October 07, 2010 9:32 AM
To: histonet-boun...@lists.utsouthwestern.edu;
Histonet@lists.utsouthwestern.edu
Subject: [Histonet] problems with staining IHC

Hi All,

Our pathologists have made a complain that the staining of slides have been
a problem.  Same antibodies which stain one day does not work the following
day.  This has been going on for a few months.  When we repeat stain they
either work or not work and we have been sending them to reference labs. 

Our tech support person was here and told us that the slides ( fisher plus
slides) have been a problem with some of her customers.  Meanwhile our
surrounding labs which are using the same slides have no issues.  She showed
us how the reagents were not spreading properly on the slides. 

Is anyone confronted this issue?  If so,  how was it solved? 

Thanks in advance.

Mala Srishan
Supervisor, Histology
Holy Name Medical Center
Teaneck NJ 07666


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Holy Name Medical Center is the recipient of:

Magnet Recognition for Excellence in Patient Care, American Nurses
Credentialing Center

100 Best Places to Work in Healthcare, Ranked Fourth Nationally by Modern
Healthcare

Best Places to Work in New Jersey, NJBIZ

Awards for Emergency, Outpatient and Inpatient Service Excellence, J.D. 
Power

Distinguished Hospital Awards for Clinical Excellence, HealthGrades

Excellence Awards for Stroke, Gastrointestinal and Pulmonary Care,
HealthGrades

Best in Value Award, Data Advantage, LLC

Chest Pain Center Accreditation, Society of Chest Pain Centers

Primary Stroke Center Designation, The Joint Commission and NJ Department of
Health and Human Services


 Warning: The information contained in this message is privileged and 
CONFIDENTIAL and is intended only for the use of the addressee above. If 
you are not the intended recipient, you are hereby notified that any 
disclosure, copying, distribution, or taking of any action in reliance on 
the content of this message is strictly prohibited. If you have received 
this communication in error, please notify the sender by replying to this 
message, and then delete it from your system.




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[Histonet] Equipment Purchase Questions

2010-10-07 Thread Cruise, Karen
Hello Histo  Community,
 We are currently looking to purchase several items. I'm hoping someone can 
shed light on whether or not we are headed in the right direction.
Processor: Initially we were leaning towards the Leica ASP 300, now I'm 
wondering if we are about to purchase to much processor for the needs of our 
lab. We process maybe 50 blocks per month. We are unable to use a microwave 
processor. We process about 95% breast tissue. Someone mentioned the TP1020. 
Has anyone any comments on this processor.
 
We are also looking to purchase a ph meter and a fume adsorber, any 
recommendations ?
Your responses will be greatly appreciated as we are looking to purchase before 
the end of the month.
 
Thanks for all your help and suggestions,
Karen
 
 
 
Karen E. Cruise
Histologist / Research Technician II
Washington University School of Medicine
Laboratory for Translational Pathology
216 S. Kingshighway Rm #2332
St Louis, MO 63110
314-454-8636 Office
314-454-5525 Fax
kcru...@path.wustl.edu
 
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RE: [Histonet] Equipment Purchase Questions

2010-10-07 Thread Feher, Stephen
Karen,

I would highly recommend Leica's Peloris processor.  We use it for rapid
tissue processing (2 hour processing time for cores and small
specimens).  It gives us the option of using one retort for rapid
processing and the other for more conventional processing.  We are also
saving on reagents since we do not have to change out the entire
processor weekly or twice per week.  Peloris keeps track of the reagents
and lets us know when one of them needs to be changed.

We have been using our two units for a little over 9 months and we have
yet to have anything either over or under processed. 


Steve

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Cruise,
Karen
Sent: Thursday, October 07, 2010 12:09 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Equipment Purchase Questions

Hello Histo  Community,
 We are currently looking to purchase several items. I'm hoping someone
can shed light on whether or not we are headed in the right direction.
Processor: Initially we were leaning towards the Leica ASP 300, now I'm
wondering if we are about to purchase to much processor for the needs of
our lab. We process maybe 50 blocks per month. We are unable to use a
microwave processor. We process about 95% breast tissue. Someone
mentioned the TP1020. Has anyone any comments on this processor.
 
We are also looking to purchase a ph meter and a fume adsorber, any
recommendations ?
Your responses will be greatly appreciated as we are looking to purchase
before the end of the month.
 
Thanks for all your help and suggestions, Karen
 
 
 
Karen E. Cruise
Histologist / Research Technician II
Washington University School of Medicine Laboratory for Translational
Pathology
216 S. Kingshighway Rm #2332
St Louis, MO 63110
314-454-8636 Office
314-454-5525 Fax
kcru...@path.wustl.edu
 
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RE: [Histonet] Equipment Purchase Questions

2010-10-07 Thread Mahoney,Janice A
I completely agree with Steve.
Jan M
Omaha

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Feher, Stephen
Sent: Thursday, October 07, 2010 11:21 AM
To: Cruise, Karen; histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] Equipment Purchase Questions

Karen,

I would highly recommend Leica's Peloris processor.  We use it for rapid
tissue processing (2 hour processing time for cores and small
specimens).  It gives us the option of using one retort for rapid
processing and the other for more conventional processing.  We are also
saving on reagents since we do not have to change out the entire
processor weekly or twice per week.  Peloris keeps track of the reagents
and lets us know when one of them needs to be changed.

We have been using our two units for a little over 9 months and we have
yet to have anything either over or under processed.


Steve

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Cruise,
Karen
Sent: Thursday, October 07, 2010 12:09 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Equipment Purchase Questions

Hello Histo  Community,
 We are currently looking to purchase several items. I'm hoping someone
can shed light on whether or not we are headed in the right direction.
Processor: Initially we were leaning towards the Leica ASP 300, now I'm
wondering if we are about to purchase to much processor for the needs of
our lab. We process maybe 50 blocks per month. We are unable to use a
microwave processor. We process about 95% breast tissue. Someone
mentioned the TP1020. Has anyone any comments on this processor.

We are also looking to purchase a ph meter and a fume adsorber, any
recommendations ?
Your responses will be greatly appreciated as we are looking to purchase
before the end of the month.

Thanks for all your help and suggestions, Karen



Karen E. Cruise
Histologist / Research Technician II
Washington University School of Medicine Laboratory for Translational
Pathology
216 S. Kingshighway Rm #2332
St Louis, MO 63110
314-454-8636 Office
314-454-5525 Fax
kcru...@path.wustl.edu

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RE: [Histonet] Equipment Purchase Questions

2010-10-07 Thread Mike Pence
I third that! I have had my Peloris for about 2 years. The key is thin,
uniform sections.

Mike

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of
Mahoney,Janice A
Sent: Thursday, October 07, 2010 11:24 AM
To: 'Feher, Stephen'; Cruise, Karen; histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] Equipment Purchase Questions


I completely agree with Steve.
Jan M
Omaha

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Feher,
Stephen
Sent: Thursday, October 07, 2010 11:21 AM
To: Cruise, Karen; histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] Equipment Purchase Questions

Karen,

I would highly recommend Leica's Peloris processor.  We use it for rapid
tissue processing (2 hour processing time for cores and small
specimens).  It gives us the option of using one retort for rapid
processing and the other for more conventional processing.  We are also
saving on reagents since we do not have to change out the entire
processor weekly or twice per week.  Peloris keeps track of the reagents
and lets us know when one of them needs to be changed.

We have been using our two units for a little over 9 months and we have
yet to have anything either over or under processed.


Steve

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Cruise,
Karen
Sent: Thursday, October 07, 2010 12:09 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Equipment Purchase Questions

Hello Histo  Community,
 We are currently looking to purchase several items. I'm hoping someone
can shed light on whether or not we are headed in the right direction.
Processor: Initially we were leaning towards the Leica ASP 300, now I'm
wondering if we are about to purchase to much processor for the needs of
our lab. We process maybe 50 blocks per month. We are unable to use a
microwave processor. We process about 95% breast tissue. Someone
mentioned the TP1020. Has anyone any comments on this processor.

We are also looking to purchase a ph meter and a fume adsorber, any
recommendations ? Your responses will be greatly appreciated as we are
looking to purchase before the end of the month.

Thanks for all your help and suggestions, Karen



Karen E. Cruise
Histologist / Research Technician II
Washington University School of Medicine Laboratory for Translational
Pathology 216 S. Kingshighway Rm #2332 St Louis, MO 63110 314-454-8636
Office 314-454-5525 Fax kcru...@path.wustl.edu

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Sponsored by Catholic Health Initiatives and Immanuel, Alegent Health is
faithful to the healing ministry of Jesus Christ, providing high quality
care for the body, mind and spirit of every person.

The information contained in this communication, including attachments,
is confidential and private and intended only for the use of the
addressees.  Unauthorized use, disclosure, distribution or copying is
strictly prohibited and may be unlawful.  If you received this
communication in error, please inform us of the erroneous delivery by
return e-mail message from your computer.  Additionally, although all
attachments have been scanned at the source for viruses, the recipient
should check any attachments for the presence of viruses before opening.
Alegent Health accepts no liability for any damage caused by any virus
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RE: [Histonet] problems with staining IHC

2010-10-07 Thread Esparza, Sandra
If Erie is the manufacture of your Fisher slides then yes we have had
the same problem with our IHC's.  We use the Ventana Benchmark and have
had this problem off and on for about 8 months.  There seems to be no
consistency with the quality of slides from Erie.  We have just switched
to the TruBond 200 slides which are distributed by STATLABS.  These are
working great for our IHC's.

Sandra
Sandra Esparza HT(ASCP)QIHC
Lead Technologist
Dell Children's Medical Center of Central Texas
512-324-  x87061
sespa...@seton.org


-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Tim
Higgins
Sent: Thursday, October 07, 2010 10:53 AM
To: sris...@mail.holyname.org;
histonet-boun...@lists.utsouthwestern.edu;
Histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] problems with staining IHC

Hi Mala,

We've used the Fisher superfrost plus slides for years and have never
had
that issue, it sounds more like you need to add some Tween to your
buffer.
That will help the solutions spread along your slide.

Hope that helps. 


Thanks,
 
Timothy Higgins, HT(ASCP) QIHC

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of
sris...@mail.holyname.org
Sent: Thursday, October 07, 2010 9:32 AM
To: histonet-boun...@lists.utsouthwestern.edu;
Histonet@lists.utsouthwestern.edu
Subject: [Histonet] problems with staining IHC

Hi All,

Our pathologists have made a complain that the staining of slides have
been
a problem.  Same antibodies which stain one day does not work the
following
day.  This has been going on for a few months.  When we repeat stain
they
either work or not work and we have been sending them to reference labs.


Our tech support person was here and told us that the slides ( fisher
plus
slides) have been a problem with some of her customers.  Meanwhile our
surrounding labs which are using the same slides have no issues.  She
showed
us how the reagents were not spreading properly on the slides. 

Is anyone confronted this issue?  If so,  how was it solved? 

Thanks in advance.

Mala Srishan
Supervisor, Histology
Holy Name Medical Center
Teaneck NJ 07666


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[Histonet] Coverslip Film

2010-10-07 Thread Paula Lucas
Hello 

Does anyone use a non-Sakura coverslip film on your Sakura coverslipper?  My
boss handed me a flyer from a company that sells film and it's a lot less
money than the Sakura brand.

 

Thanks,

Paula

Lab Manager

Path Lab

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[Histonet] Responses

2010-10-07 Thread Cruise, Karen
Thanks so much for your quick responses .Let me elaborate on my specific needs. 
We are a research lab that deals mainly with breast tissue. I have been led to 
believe that microwave processing may not be the way to go because of our 
specimens are  being used for RNA and DNA studies. A quick turn around time is 
not a concern of ours since we process and hold specimens for future use based 
upon requests throughout the US. Our main concern is not purchasing more 
processor than what we need since we only process maybe 5-10 cassettes per week.
 
Thanks again,
Karen
 
Karen E. Cruise
Histologist / Research Technician II
Washington University School of Medicine
Laboratory for Translational Pathology
216 S. Kingshighway Rm #2332
St Louis, MO 63110
314-454-8636 Office
314-454-5525 Fax
kcru...@path.wustl.edu
 
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[Histonet] p16 antibody

2010-10-07 Thread Michele Carr
Hello all I am relatively new to IHC and my pathologist is requesting the p16 
antibody, I have not been able to find it at any of the vendors we work with. I 
did a google search and saw that MTM labs has it but it seems as though they 
sell it as a kit. Does anyone know where I could find this antibody that I 
could 
use on the bond autostaining machine. Thank you,
Michele Carr HTL ASCP
Medical Laboratory Services
Murrieta Ca


  
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RE: [Histonet] p16 antibody

2010-10-07 Thread McMahon, Loralee A
If you want the IVD form of the antibody you have to go with MTM labs, they 
hold the patent.  We buy the kit and take out the antibody and use the 
detection for research.   It works very very well.  


Loralee McMahon, HTL (ASCP)
Immunohistochemistry Supervisor
Strong Memorial Hospital
Department of Surgical Pathology
(585) 275-7210

From: histonet-boun...@lists.utsouthwestern.edu 
[histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Michele Carr 
[michelecar...@yahoo.com]
Sent: Thursday, October 07, 2010 1:15 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] p16 antibody

Hello all I am relatively new to IHC and my pathologist is requesting the p16
antibody, I have not been able to find it at any of the vendors we work with. I
did a google search and saw that MTM labs has it but it seems as though they
sell it as a kit. Does anyone know where I could find this antibody that I could
use on the bond autostaining machine. Thank you,
Michele Carr HTL ASCP
Medical Laboratory Services
Murrieta Ca



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RE: [Histonet] p16 antibody

2010-10-07 Thread Settembre, Dana
Hi Michele,
Yes, it's true, only MTM labs sells it and they
Sell it as a kit and they also 
sell it along with a negative control reagent.
That's how I buy it.
They have a license or something and no else can sell it now.
Their cat# is 9518 and I think it's called the 
CINteck Histology V-kit,
(you should double check with them.)
They will make you open up an account...

Good Luck
Dana Settembre
University Hospital - UMDNJ
Newark, NJ



-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Michele Carr
Sent: Thursday, October 07, 2010 1:16 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] p16 antibody

Hello all I am relatively new to IHC and my pathologist is requesting the p16 
antibody, I have not been able to find it at any of the vendors we work with. I 
did a google search and saw that MTM labs has it but it seems as though they 
sell it as a kit. Does anyone know where I could find this antibody that I 
could 
use on the bond autostaining machine. Thank you,
Michele Carr HTL ASCP
Medical Laboratory Services
Murrieta Ca


  
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[Histonet] RE: Histonet Digest, Vol 83, Issue 8

2010-10-07 Thread Joanne Clark
Another consideration as a few have mentioned could be with your
automated stainer (if you use one).  We have a DAKO autostainer and we
found our staining had become very sporadic.  When I did a repeat run
manually, everything was beautiful.  We found that a pump on the stainer
was going and it wasn't washing all the reagents off the slide between
steps.  In addition the probe needed to be replaced as it was drawing up
air into the lines and the volumes it was dispensing on the slides was
variable from slide to slide depending on how much air was in the probe
lines at any given time.  If you do use automation, when was the last
time the machine had a PM?  I agree with the others that tween in your
wash buffer is a must.

Joanne Clark, HT
Pathology Consultants of New Mexico

--

Message: 1
Date: Thu, 7 Oct 2010 07:32:13 -0700
From: sris...@mail.holyname.org
Subject: [Histonet] problems with staining IHC
To: histonet-boun...@lists.utsouthwestern.edu,
Histonet@lists.utsouthwestern.edu
Message-ID:

of6e74eb3d.a17b453b-on852577b5.004f018d-882577b5.005f9...@holyname.org

Content-Type: text/plain; charset=US-ASCII

Hi All,

Our pathologists have made a complain that the staining of slides have 
been a problem.  Same antibodies which stain one day does not work the 
following day.  This has been going on for a few months.  When we repeat

stain they either work or not work and we have been sending them to 
reference labs. 

Our tech support person was here and told us that the slides ( fisher
plus 
slides) have been a problem with some of her customers.  Meanwhile our 
surrounding labs which are using the same slides have no issues.  She 
showed us how the reagents were not spreading properly on the slides. 

Is anyone confronted this issue?  If so,  how was it solved? 

Thanks in advance.

Mala Srishan
Supervisor, Histology
Holy Name Medical Center
Teaneck NJ 07666











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[Histonet] Equipment purchases responses

2010-10-07 Thread Cruise, Karen
Thanks so much for your quick responses .Let me elaborate on my specific needs. 
We are a research lab that deals mainly with breast tissue. I have been led to 
believe that microwave processing may not be the way to go because of our 
specimens are  being used for RNA and DNA studies. A quick turn around time is 
not a concern of ours since we process and hold specimens for future use based 
upon requests throughout the US. Our main concern is not purchasing more 
processor than what we need since we only process maybe 5-10 cassettes per week.
 
Thanks again,
Karen
 
 
 
 
 
Karen E. Cruise
Histologist / Research Technician II
Washington University School of Medicine
Laboratory for Translational Pathology
216 S. Kingshighway Rm #2332
St Louis, MO 63110
314-454-8636 Office
314-454-5525 Fax
kcru...@path.wustl.edu
 
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Re: [Histonet] Coverslip Film

2010-10-07 Thread Rene J Buesa
Once I tried one and it was harder, reacted less readily with xylene, and 
tended to peel-off easier. You could ask for a sample and try it.
René J.

--- On Thu, 10/7/10, Paula Lucas plu...@biopath.org wrote:


From: Paula Lucas plu...@biopath.org
Subject: [Histonet] Coverslip Film
To: histonet@lists.utsouthwestern.edu
Date: Thursday, October 7, 2010, 12:45 PM


Hello 

Does anyone use a non-Sakura coverslip film on your Sakura coverslipper?  My
boss handed me a flyer from a company that sells film and it's a lot less
money than the Sakura brand.



Thanks,

Paula

Lab Manager

Path Lab

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[Histonet] Bone IHC

2010-10-07 Thread Vanessa J. Phelan
Hi everyone,

I was wondering if anyone has any tricks on how to get bone sections to stop 
lifting off the slide through the IHC process? I leave them in the oven for 
quite a while to make sure they are baked on, however after antigen retrieval  
(pressure cooker for 20mins) most of the boney part of the tissue comes off and 
the marrow and muscle stays put! The sections are cut onto superfrost plus 
slides.

Any help would be much appreciated, thanks.

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[Histonet] ECM stain for growing cartilage

2010-10-07 Thread Liz Chlipala
Hello Everyone

 

Is anyone out there aware of an ECM stain that can be used on growing
tissue culture cells in a hydrogel.  What I'm really looking for is a
live stain I can use on the whole gel and see with a light microscope.
I want to get a general idea of the amount of ECM that is growing.  So
it could just be a general bulk ECM (proteoglycan or collagen) stain
that will show a contrast from the gel.  And I want to be able to return
the gel to the incubator and do the stain again multiple days later.  I
have searched extensively for something that would do this and I have
come up with nothing.  Any advice is appreciated and thanks in advance

 

Liz

 

Elizabeth A. Chlipala, BS, HTL(ASCP)QIHC

Manager

Premier Laboratory, LLC

PO Box 18592

Boulder, Colorado 80308

office (303) 682-3949 

fax (303) 682-9060

www.premierlab.com

 

 

Ship to Address:

1567 Skyway Drive, Unit E

Longmont, Colorado 80504

 

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RE: [Histonet] Bone IHC

2010-10-07 Thread Liz Chlipala
We lower the temp of retrieval to 70C for 2 hours and have good success
with that.

Liz

Elizabeth A. Chlipala, BS, HTL(ASCP)QIHC
Manager
Premier Laboratory, LLC
PO Box 18592
Boulder, Colorado 80308
office (303) 682-3949 
fax (303) 682-9060
www.premierlab.com
 
 
Ship to Address:
1567 Skyway Drive, Unit E
Longmont, Colorado 80504

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Vanessa
J. Phelan
Sent: Thursday, October 07, 2010 1:14 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Bone IHC

Hi everyone,

I was wondering if anyone has any tricks on how to get bone sections to
stop lifting off the slide through the IHC process? I leave them in the
oven for quite a while to make sure they are baked on, however after
antigen retrieval  (pressure cooker for 20mins) most of the boney part
of the tissue comes off and the marrow and muscle stays put! The
sections are cut onto superfrost plus slides.

Any help would be much appreciated, thanks.

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Re: [Histonet] Bone IHC

2010-10-07 Thread Rene J Buesa
If you have a bone that will require IHC, you will have to make sure that the 
Gross section is no more than 1.5 mm thick and decalcify it in EDTA. The you 
have to make sure that the infiltration is complete. These are the 2 initial 
factors.
Later you will have to section it as thin as you can, place the sections in (+) 
slides let them drain completely before going into the oven. Extra time in the 
oven is not really required if the aforementioned steps are done.
Then add enough dishwasher soap to the HIER solution to get a solution of 2% 
and you will dewax and retrieve the antigen simultaneously. The sections will 
survive to complete the IHC procedure.René J.

--- On Thu, 10/7/10, Vanessa J. Phelan vjp2...@columbia.edu wrote:



From: Vanessa J. Phelan vjp2...@columbia.edu
Subject: [Histonet] Bone IHC
To: histonet@lists.utsouthwestern.edu histonet@lists.utsouthwestern.edu
Date: Thursday, October 7, 2010, 3:13 PM


Hi everyone,

I was wondering if anyone has any tricks on how to get bone sections to stop 
lifting off the slide through the IHC process? I leave them in the oven for 
quite a while to make sure they are baked on, however after antigen retrieval  
(pressure cooker for 20mins) most of the boney part of the tissue comes off and 
the marrow and muscle stays put! The sections are cut onto superfrost plus 
slides.

Any help would be much appreciated, thanks.

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Re: [Histonet] Bone IHC

2010-10-07 Thread Adam .
I've been experimenting with different ways to solve this problem myself. I
fix my tissues in 10% zinc buffered formalin and decalcify in formic acid
for 72 hours, followed by embedding and cutting 5 uM sections.

From trial and error, I've determined that incubating the slides flat on a
slide warmer at 37C (or in my case, the bottom of an unused bacterial
incubator) can prevent nearly all the detachment you observe but it's time
dependent. I think the problem is that the sections get small amounts of
water underneath them when you scoop them up off the water surface during
sectioning and during HIER, that water boils and shears off the slide.

If you leave the slides overnight, the slides were get destroyed during
HIER. However, if you leave them for a week, they tend to be nearly
untouched even at 95C for 10 mins. I'm currently in the process of
determining if a few days is enough time.

Adam

On Thu, Oct 7, 2010 at 2:20 PM, Liz Chlipala l...@premierlab.com wrote:

 We lower the temp of retrieval to 70C for 2 hours and have good success
 with that.

 Liz

 Elizabeth A. Chlipala, BS, HTL(ASCP)QIHC
 Manager
 Premier Laboratory, LLC
 PO Box 18592
 Boulder, Colorado 80308
 office (303) 682-3949
 fax (303) 682-9060
 www.premierlab.com


 Ship to Address:
 1567 Skyway Drive, Unit E
 Longmont, Colorado 80504

 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu
 [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Vanessa
 J. Phelan
 Sent: Thursday, October 07, 2010 1:14 PM
 To: histonet@lists.utsouthwestern.edu
 Subject: [Histonet] Bone IHC

 Hi everyone,

 I was wondering if anyone has any tricks on how to get bone sections to
 stop lifting off the slide through the IHC process? I leave them in the
 oven for quite a while to make sure they are baked on, however after
 antigen retrieval  (pressure cooker for 20mins) most of the boney part
 of the tissue comes off and the marrow and muscle stays put! The
 sections are cut onto superfrost plus slides.

 Any help would be much appreciated, thanks.

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[Histonet] Histology Supervisor Job in Texas!

2010-10-07 Thread Alisha Dynan


Hi Histonet Members









 


I hope you are doing well. I am a Recruiter at a highly successful and well 
respected Healthcare recruiting firm.  I help place Lab Professionals in 
permanent positions across the country and I wanted to see if you are 
interested in exploring other career opportunities?  We are completely free of 
charge to candidates and and we work on quite a few laboratory openings across 
the country. Our clients typically assist with relocation expenses. 




 


I am currently working with a client in the Midland/Odessa Texas area to locate 
a Histology Supervisor.  This 350+ bed community teaching hospital system has a 
very strong reputation in area. My client is looking for someone who is HT or 
HTL certified, has 5 + years for histology experience, and prefers someone with 
supervisory or lead experience.  This hospital system offers a very competitive 
base salary/hourly rate, an outstanding benefits and retirement package, and 
relocation assistance.  Please email me asap if you are interested in more 
details. Email ali...@ka-recruiting.com.

 

Below is a list of some of the other opportunities we are currently working on. 
If you do not see an opening in a location in which you live or would like to 
live, please send me an email me a copy of your resume and let me know where 
you would be interested in a job. I will then tailor a search for you that is 
completely confidential and free to candidates.

 

Current Laboratory Opportunities: 

 

Histotechnologist:

1. Histotech - Syracuse NY

2. Histology Manager - Michigan

3. Histotech - NYC

4. Histology Supervisor - GA

5. Histotech - NV (Must have Bachelors Degree)

6. Nashville, TN - Histotech

7. Histotech - Cape Cod, MA

8. Histology Supervisor - TX

9. General Manager of Anatomic Pathology - NJ

 


 





















If you're interested in learning more about these opportunities or 
opportunities in a certain geographic location please reply with an updated 
resume and let me know when a good time to reach you is.  

 

If this is not the right fit for you please let me know who you can recommend 
and give me an idea of what types of positions you'd be interested in hearing 
about in the future.  I cover the entire US and have am working on Lab 
positions at all levels. We offer a very generous referral bonus for anyone you 
refer to us that we place into any position across the country.  

 


To view some additional opportunities please visit our website at 
www.ka-recruiting.com.  


























Sincerely,

 

Alisha (Taylor) Dynan, Founder

K.A. Recruiting, Inc.

Your Partner in Healthcare Recruiting

10 Post Office Square 8th Floor SOUTH

Boston, MA 02109

P: (617) 692-2949

F: (617) 507-8009

ali...@ka-recruiting.com

www.ka-recruiting.com


Sincerely,

 

Alisha (Taylor) Dynan, Founder

K.A. Recruiting, Inc.

Your Partner in Healthcare Recruiting

10 Post Office Square 8th Floor SOUTH

Boston, MA 02109

P: (617) 692-2949

F: (617) 507-8009

ali...@ka-recruiting.com

www.ka-recruiting.com

 






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[Histonet] cassette labelers

2010-10-07 Thread Robert Richmond
 I'm advising a locum tenens client of mine about acquiring a cassette
labeler. The only one I'm familiar with is Thermo Scientific's
Cassette MicroWriter. Some questions for HistoNet:

1) A JCAHO inspector informed them that a cassette labeler will soon
be required. Does anyone know if this is in fact the case?

2) Will the labeler print patients' names, or other second identifiers
such as JCAHO now requires?

3) Are these labelers available in the used instrument market?

4) Is there any competition, or is the Thermo product all there is?

5) How well do these labelers withstand use?

Bob Richmond
Samurai Pathologist
Knoxville TN

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RE: [Histonet] Equipment purchases responses

2010-10-07 Thread Hugh Luk







Hi Karen,

I am in a the same Research situation as you.  If you are sure that all you 
will need is small (100) tissue cassette processings, the Leica TP1020 should 
suffice.  We call them Dip-and-Dunks, as the tissue carousels from bucket to 
bucket.  It is economical on reagents and is easy to use.  Plan on 12+ hour 
processing runs for tissue with fat.  Get the extra paraffin bucket (3) if you 
can.  It is not a necessity for the routine processing run, but it is 'Handy' 
to have.

However for fatty tissues like breast, the tissue processing is superior in 
vacuum infiltration units like the Leica ASP300S or a Tissue Tek VIP series.  
If you have the money, I recommend one of these.  Both are work-horses and will 
give you practically no trouble.  However, you will hear new terms like Warm 
Water Flush, Clean the Retort, and Annual preventive maintenance.  You 
will also triple your Waste reagents compared to the TP1020.

I have a Leica ASP300.  It was a refurbished unit, which I regret every so 
often, but it was necessary to procure due to money and time.  Mostly money.  
It has saved my bu** more often than not.  I can offer some recommendations for 
vendors like this if you wish.  I also have access to the TP1020, ASP300S, 
Peloris, and the Tissue Teks 300, 5, and 6.  

I prefer the Tissue Tek 6, but all units have worked well for me.

I have read other recommendations for the Leica Peloris or some variety of 
microwave tissue processor.  These processors are absolutely fantastic and 
fast, but I have the same red-flags as you with RNA/DNA damage.No 
microwaves.  The Peloris, in theory, will not cause further RNA/DNA damage, but 
it is advertised as Faster Than Microwaves, so I would use caution pursuing 
this model until someone documents what it is doing to the nucleotides.  Also, 
the Peloris is more expensive and it's 600 block capacity is too big for my 
(your?) needs.

As for your portable fume hood and pH meter.  pH meters range from cheap to 
super-expensive.  The pocket version is cheap but falls into disrepair quickly. 
 The bench-top models, requiring pH Standard calibrations and probe care, are 
great, but a pain to maintain and expensive to buy.   You need to define what 
you need it for.  Translational Pathology?  Perhaps you can borrow?  It seems 
to be a waste to have an expensive pH meter if (for example) you only measure 
buffers once a week.  We have a Checkmate from Cardinal scientific, but I think 
this model has been discontinued.

 Fume hood; If you cannot get your facilities folks to put a real hood in, try 
Labconco or Thermo.  Get one that can be used as a Laminar Flow (air filter 
parallel to desk), as formalin and xylene fumes lay close to the desk-top.  
There are lots of brands with different kinds and sizes of hoods.  I believe 
that filtered hoods are not very efficient at cleaning the air of formalin 
(potassium permanganate filter) or xylene (carbon), simply because there is not 
enough air exchange.   An example of our 36x24x30 self contained hood is in 
the link below:
http://www.vwrsp.com/catalog/product/index.cgi?catalog_number=82010-736inE=1highlight=82010-736

Hope this helps,


Hugh
Luk, HTL (ASCP)

Pathology shared resource lab manager

1236 Lauhala street, 
Honolulu, HI 96813








 Date: Thu, 7 Oct 2010 13:00:47 -0500
 From: kcru...@path.wustl.edu
 To: histonet@lists.utsouthwestern.edu
 Subject: [Histonet] Equipment purchases responses
 
 Thanks so much for your quick responses .Let me elaborate on my specific 
 needs. We are a research lab that deals mainly with breast tissue. I have 
 been led to believe that microwave processing may not be the way to go 
 because of our specimens are  being used for RNA and DNA studies. A quick 
 turn around time is not a concern of ours since we process and hold specimens 
 for future use based upon requests throughout the US. Our main concern is not 
 purchasing more processor than what we need since we only process maybe 5-10 
 cassettes per week.
  
 Thanks again,
 Karen
  
  
  
  
  
 Karen E. Cruise
 Histologist / Research Technician II
 Washington University School of Medicine
 Laboratory for Translational Pathology
 216 S. Kingshighway Rm #2332
 St Louis, MO 63110
 314-454-8636 Office
 314-454-5525 Fax
 kcru...@path.wustl.edu
  
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